Stryker recalls specific end cap implants due to potential blister pack compromise affecting sterility. This could lead to infection if used improperly.
Seal integrity of the blister pack may be compromised and sterility cannot be assured
Stryker is recalling certain end cap implants for potential blister pack compromise that might compromise sterility. Using these implants could lead to infection if not handled properly.
The blister pack may be compromised, which could allow contamination and reduce sterility. This poses a risk of infection if the implant is used without proper sterility assurance.
Patients who received the recalled end caps (catalog number 18300003S) during surgery. Surgeons and medical staff using these implants are most at risk.
Check for the catalog number 18300003S on the end cap. The product is used for single-use bone fixation in surgeries.
Look for the catalog number 18300003S on the end cap to confirm if it is recalled.
The recall indicates potential sterility issues, so it is not recommended for use without confirming it is not recalled.
Check the catalog number 18300003S to see if it is recalled; if yes, contact Stryker for guidance.
The recall record does not specify a replacement option.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2376-2020 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2376-2020 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
